Reliability and validity of the International Cooperative Ataxia Rating Scale: a study in 156 spinocerebellar ataxia patients. - Wikidata - wikimedia - TriplyDB

Reliability and validity of the International Cooperative Ataxia Rating Scale: a study in 156 spinocerebellar ataxia patients.

Reliability and validity of the International Cooperative Ataxia Rating Scale: a study in 156 spinocerebellar ataxia patients.

http://www.wikidata.org/entity/Q34490303

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Intra-erythrocyte infusion of dexamethasone reduces neurological symptoms in ataxia teleangiectasia patients: results of a phase 2 trial Spastic paraplegia type 7 is associated with multiple mitochondrial DNA deletions The effects of sleep dysfunction on cognition, affect, and quality of life in individuals with cerebellar ataxia.A toolbox to visually explore cerebellar shape changes in cerebellar disease and dysfunction.Longitudinal tracking of gait and balance impairments in cerebellar disease Neuropsychological features of patients with spinocerebellar ataxia (SCA) types 1, 2, 3, and 6.A randomized trial of oral betamethasone to reduce ataxia symptoms in ataxia telangiectasia.Cognition is only minimally impaired in Spinocerebellar ataxia type 14 (SCA14): a neuropsychological study of ten Norwegian subjects compared to intrafamilial controls and population norm.Autosomal dominant hereditary ataxia in Sri Lanka.Development of a brief ataxia rating scale (BARS) based on a modified form of the ICARS.Force dysmetria in spinocerebellar ataxia 6 correlates with functional capacity Change in the cortical complexity of spinocerebellar ataxia type 3 appears earlier than clinical symptoms Rating disease progression of Friedreich's ataxia by the International Cooperative Ataxia Rating Scale: analysis of a 603-patient database.MRI-based cerebellar volume measurements correlate with the International Cooperative Ataxia Rating Scale score in patients with spinocerebellar degeneration or multiple system atrophy.Ataxia rating scales--psychometric profiles, natural history and their application in clinical trials.Systematic review of the psychometric properties of balance measures for cerebellar ataxia.Rehabilitation for Individuals With Genetic Degenerative Ataxia: A Systematic Review.Annual change in Friedreich's ataxia evaluated by the Scale for the Assessment and Rating of Ataxia (SARA) is independent of disease severity.Dynamic balance in children with attention-deficit hyperactivity disorder and its relationship with cognitive functions and cerebellum.Evaluation and treatment of Langerhans cell histiocytosis patients with central nervous system abnormalities: Current views and new vistas.Cognitive and affective impairments of a novel SCA/MND crossroad mutation Asidan.The effect of piracetam on ataxia: clinical observations in a group of autosomal dominant cerebellar ataxia patients.Ataxia rating scales are age-dependent in healthy children.Effects of different exercise modalities on ataxia in multiple sclerosis patients: a randomized controlled study.Specific influences of cerebellar dysfunctions on gait.Monitoring disease progression in spinocerebellar ataxias: implications for treatment and clinical research.Reliability and discriminant validity of ataxia rating scales in early onset ataxia.High Serum GFAP Levels in SCA3/MJD May Not Correlate with Disease Progression.Neocortical atrophy in Machado-Joseph disease: a longitudinal neuroimaging study.SCA14 in Norway, two families with autosomal dominant cerebellar ataxia and a novel mutation in the PRKCG gene.Linking coordinative and executive dysfunctions to atrophy in spinocerebellar ataxia 2 patients.Spinocerebellar ataxia type 2: Measures of saccade changes improve power for clinical trials.A founder mutation p.H701P identified as a major cause of SPG7 in Norway.A neurological examination score for the assessment of spinocerebellar ataxia 3 (SCA3)

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Reliability and validity of the International Cooperative Ataxia Rating Scale: a study in 156 spinocerebellar ataxia patients.

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